Sobreiro Mariana Alves, Della Torre Adriana, de Araújo Maria Elisa Melo Branco, Canella Paula Renata Bueno Campos, de Carvalho João Ernesto, Carvalho Patrícia de Oliveira, Ruiz Ana Lucia Tasca Gois
Health Sciences Postgraduate Program, Universidade São Francisco (USF), Bragança Paulista 12916-900, SP, Brazil.
Laboratory of Phytochemistry and Experimental Pharmacology and Toxicology (LAFTEX), Faculty of Pharmaceutical Sciences, University of Campinas, 200 Candido Portinari Street, Campinas 13083-871, SP, Brazil.
Life (Basel). 2023 Feb 16;13(2):549. doi: 10.3390/life13020549.
The bioavailability of glucoside flavonoids is influenced by the nature of the sugar, glucosides being absorbed faster than rhamnoglucosides, for example. One strategy to enhance the bioavailability is enzymatic hydrolysis. In this study, some kinetic parameters of hesperidinase-mediated hydrolysis of rutin were evaluated using an UHPLC/QTOF-MS analysis of the products of a bioconversion reaction. The resulting hydrolyzed rutins (after 4, 8 and 12 h of reaction) were submitted to anti-proliferative and Cytokinesis-Block Micronucleus (CBMN) assays in CHO-K1 cells. In the hesperidinase-mediated hydrolysis, the final concentration of quercetin-3-O-glucoside (Q3G) was directly proportional to the rutin concentration and inversely proportional to the reaction time. At an anti-proliferative concentration (2.5 μg/mL), hydrolyzed rutin derivatives did not show a mutagenic effect, except for the sample with a higher content of Q3G (after 4 h of the enzymatic hydrolysis of rutin). Moreover, the higher Q3G content in hydrolyzed rutin protected the CHO-K1 cells 92% of the time against methyl methanesulfonate-induced mutagenic damage. These results suggested that the anti-mutagenic effect of hydrolyzed rutin might be related to antioxidant and cell death induction. Presenting a good lipophilicity/hydrophilicity ratio, together with antioxidant and anti-mutagenic activities, the hesperidinase-mediated hydrolyzed rutin seemed to be a promisor raw material for the development of food supplements.
糖苷类黄酮的生物利用度受糖的性质影响,例如,葡萄糖苷的吸收速度比鼠李糖苷快。提高生物利用度的一种策略是酶促水解。在本研究中,使用超高效液相色谱/四极杆飞行时间质谱(UHPLC/QTOF-MS)分析生物转化反应产物,评估了橙皮苷酶介导的芦丁水解的一些动力学参数。将所得水解芦丁(反应4、8和12小时后)在CHO-K1细胞中进行抗增殖和细胞阻滞微核(CBMN)试验。在橙皮苷酶介导的水解中,槲皮素-3-O-葡萄糖苷(Q3G)的最终浓度与芦丁浓度成正比,与反应时间成反比。在抗增殖浓度(2.5μg/mL)下,水解芦丁衍生物除了芦丁酶促水解4小时后Q3G含量较高的样品外,未显示出诱变作用。此外,水解芦丁中较高的Q3G含量在92%的时间内保护CHO-K1细胞免受甲磺酸甲酯诱导的诱变损伤。这些结果表明,水解芦丁的抗诱变作用可能与抗氧化和诱导细胞死亡有关。由于具有良好的亲脂性/亲水性比例,以及抗氧化和抗诱变活性,橙皮苷酶介导的水解芦丁似乎是开发食品补充剂的一种有前途的原料。